back to PRO homepage
  Home |   Linked Open Data |   Browse |  
Search

|   Statistics |   Download
 RACE-PRO
 PRO tracker
 Community
 PRO Consortium
 Publications
 Documentation

Protein Ontology report - cystic fibrosis transmembrane conductance regulator (human)
PR:P13569 - http://purl.obolibrary.org/obo/PR_P13569
 
  Protein Forms  Annotations      
Ontology Information Show OBO stanza / PAF / GPI
  PRO ID
PR:P13569   
  PRO namecystic fibrosis transmembrane conductance regulator (human) 
  Synonyms
PRO-Short-label: EXACT:hCFTR
Gene-based: RELATED:ABCC7 | CFTR
Other: EXACT:ATP-binding cassette sub-family C member 7 (human) | cAMP-dependent chloride channel (human) | channel conductance-controlling ATPase (human)
  Definition"A cystic fibrosis transmembrane conductance regulator that is encoded in the genome of human." [PRO:CNA, UniProtKB:P13569
  PRO Categoryorganism-gene 
  ParentPR:000001044
PR:000029067
  Gene TemplateHGNC:1884 CFTR (human)
  TaxonNCBITaxon:9606 Homo sapiens
  Terms by PRO Category
Organism-Independent Organism-Specific
         Category          Number of Terms          Category          Number of Terms
         Gene0                                                  Organism-Gene 1                                        
         Sequence0                                                  Organism-Sequence 5                                        
         Modification0                                                  Organism-Modification 5                                        
  Term Hierarchy
  Visualization
DAG: OLS:
Back to top
Related Cross References

  Db identifiers
UniProtKB:P13569
Back to top
Protein Forms  Switch to Extended View   

Category  

PRO Form Name

Ann. Has Annotation?

Comp. In Complex?
organism-gene



PR:P13569 cystic fibrosis transmembrane conductance regulator (human), hCFTR


organism-sequence



PR:000063429 cystic fibrosis transmembrane conductance regulator sequence variant N1303K (human), hCFTR/var:N1303K


organism-sequence



PR:000063523 cystic fibrosis transmembrane conductance regulator sequence variant G551D (human), hCFTR/var:G551D


organism-sequence



PR:P13569-1 cystic fibrosis transmembrane conductance regulator isoform 1 (human), hCFTR/iso:1


organism-modification



PR:000036593 cftr isoform 1 N-glycosylated 1 (human), hCFTR/iso:1/NGlyco:1


organism-modification



PR:000036594 cftr isoform 1 phosphorylated 1 (human), hCFTR/iso:1/Phos:1

Yes

organism-modification



PR:000036595 cftr isoform 1 phosphorylated 2 (human), hCFTR/iso:1/Phos:2


organism-sequence



PR:P13569-2 cystic fibrosis transmembrane conductance regulator isoform 2 (human), hCFTR/iso:2


organism-sequence



PR:P13569-3 cystic fibrosis transmembrane conductance regulator isoform 3 (human), hCFTR/iso:3

Yes

organism-modification



PR:000046699 cystic fibrosis transmembrane conductance regulator ubiquitinated form (human), hCFTR/UbiqLys+


organism-modification



PR:000079746 cystic fibrosis transmembrane conductance regulator phosphorylated 1 (human), hCFTR/Phos:1


Back to top
Functional Annotation (PRO-centric view) Switch to GO Centric View   
PRO Term GO Annotation Evidence
PR:000036594
hCFTR/iso:1/Phos:1
UniProtKB:P13569-1, Ser-737/Ser-768/Ser-795/Ser-813, MOD:00046
enablesGO:0005260 intracellularly ATP-gated chloride channel activity PMID:1716180
GO:0005260 intracellularly ATP-gated chloride channel activity PMID:1716180
PR:P13569-3
hCFTR/iso:3
associated_with_disease_progressionDO:1485 cystic fibrosis PMID:12913074